Zydus Lifesciences receives tentative USFDA approval for Letermovir tablets

Zydus Lifesciences Ltd has received tentative approval from the United States Food and Drug Administration (USFDA) to market Letermovir tablets, 240 mg and 480 mg.

Letermovir tablets are used to prevent disease caused by a virus called cytomegalovirus (CMV) in people who have received a bone marrow transplant or kidney transplant. The drug will be manufactured at the group’s formulation manufacturing facility at Ahmedabad SEZ, the company said in a stock exchange filing.

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Letermovir tablets, 240 mg and 480 mg, had annual sales of $289.5 million in the US. The group now has 393 approvals and has so far filed over 460 ANDAs since the commencement of the filing process in FY 2003-04, the company added.

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